FLEXLENS(METHAFILCON A)— 510(k) K962000

Substantially Equivalent

Flexlens, Inc.

FDA 510(k) clearance K962000 for FLEXLENS(METHAFILCON A), Substantially Equivalent on 1996-10-01. Applicant: Flexlens, Inc..

Clearance details

Applicant: Flexlens, Inc.
Product code: Code LPL
Advisory panel: Ophthalmic
Date received: 1996-05-22
Decision date: 1996-10-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Roswell, GA, US

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Adverse events under product code LPL

product code LPL

Injury: 988
Other: 4
Total: 992

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.